不同基质降解物的共价连接控制了DegP蛋白质的组装和拆卸
Seokhee Kim1, Robert A Grant, Robert T Sauer
1Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Cell
|April 5, 2011
概括
蛋白质质量控制依赖于DegP蛋白酶激活. 连接的基质降解子驱动活跃的DegP子的组装,在蛋白质降解完成后,这些子分解,确保精确的蛋白质分解.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 结构生物学 结构生物学
背景情况:
- 蛋白质质量控制对于细胞功能至关重要.
- 周等离子体蛋白酶DegP通过组装成活性来调节蛋白质分解.
- 激活DegP是由基质结合触发的.
研究的目的:
- 阐明DegP激活和子组装的机制.
- 为了研究基质序列在DegP函数中的作用.
- 了解蛋白质分解活性对基质可用性的调节.
主要方法:
- 基质结合的DegP十二相体的X射线晶体学.
- 福斯特共振能量转移 (FRET) 实验.
- 对基质降解子与DegP相互作用的分析.
主要成果:
- DegP的激活需要对不同的基质降解子进行共价连接.
- 一个degron结合了活性部位,另一个结合了PDZ1结合部位.
- 活以合作方式组装,在降解过程中保持稳定,并在基质耗尽时拆卸.
结论:
- 基板降解结合能量驱动蛋白质溶解机组件.
- 只有当有足够的基质存在时,DegP才会活跃,从而确保调节的蛋白质分解.
- 这种机制为蛋白质质量控制提供了一个敏感的反循环.
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